Viewing Study NCT00909857


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Study NCT ID: NCT00909857
Status: COMPLETED
Last Update Posted: 2015-08-24
First Post: 2009-04-24
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Effect on Primary Dysmenorrhea
Sponsor: Bayer
Organization:

Study Overview

Official Title: A Multi-center, Double-blind, Double-dummy, Randomized, Controlled, Parallel-group Study to Assess Efficacy and Safety of SH T00658ID Compared to SH D593B in the Treatment of Primary Dysmenorrhea
Status: COMPLETED
Status Verified Date: 2015-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To investigate the potential benefits of a new oral contraceptive (SH T00658ID) on alleviating complaints of dysmenorrhea associated with oral contraceptive use.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2008-005625-11 EUDRACT_NUMBER None View
312042 OTHER Bayer View